RS28933068 FGFR3
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What This Variant Does
"[OMIM:HYPOCHONDROPLASIA]
Associated Conditions
Hypochondroplasia
Achondroplasia
Neurodevelopmental delay
FGFR3-related disorder
FGFR3-related chondrodysplasia
Inborn genetic diseases
Hypochondroplasia
Short stature
Inborn genetic diseases
14 conditions
Achondroplasia
Larsen syndrome
Connective tissue disorder
FGFR3-related disorder
Hypochondroplasia
Other Variants in FGFR3